Amphoteric trap modeling of multidielectric scaled SONOS nonvolatile memory structures

We have characterized multidielectric scaled SONOS nonvolatile memory structures with the quasi-static linear voltage ramp (LVR) technique and dynamic pulse measurements. We have formulated physically-based ERASE/WRITE and retention methods with deep level amphoteric traps which capture and emit carriers to the bands in the silicon nitride film. Amphoteric trap parameters are extracted by the LVR technique. ERASE/WRITE and retention amphoteric trap model simulations agree well with the experimental dynamic pulse measurements. Experimental scaled SONOS structures have been fabricated with tunnel oxide X_OT=20 Å, nitride X_N=30 Å and blocking oxide X_OB=55 Å and demonstrated a static flatband shift of 3.6 V with ±5 V programming voltages. These structures may be used as the nonvolatile memory element in high density VLSI circuits.     

Aeroelastic flutter of a disk rotating in an unbounded acoustic medium

The linear aeroelastic stability of an unbaffled flexible disk rotating in an unbounded fluid is investigated by modeling the disk-fluid system as a rotating Kirchhoff plate coupled to the irrotational motions of a compressible inviscid fluid. A perturbed eigenvalue formulation is used to compute systematically the coupled system eigenvalues. Both a semi-analytical and a numerical method are employed to solve the fluid boundary value problem. The semi-analytical approach involves a perturbation series solution of the dual integral equations arising from the fluid boundary value problem. The numerical approach is a boundary element method based on the Hadamard finite part. Unlike previous works, it is found that a disk with zero material damping destabilizes immediately beyond its lowest critical speed. Upon the inclusion of small disk material damping, the flutter speeds become supercritical and increase with decreasing fluid density. The competing effects of radiation damping into the surrounding fluid and disk material damping control the onset of flutter at supercritical speed. The results are expected to be relevant for the design of rotating disk systems in data storage, turbomachinery and manufacturing applications.     

Extending Coggia–Couvreur attack on Loidreau’s rank-metric cryptosystem

Designs, Codes and Cryptography - A recent paper by Coggia and Couvreur presents a polynomial time key-recovery attack on Loidreau’s encryption scheme, based on rank-metric codes, for some...     

A facile synthesis of natural products chaetomellic acid A and 1,7(Z)- nonadecadiene-2,3-dicarboxylic acid

Synthesis of recently isolated bioactive natural products chaetomellic acid A anhydride (1) and a novel 1,7(Z)-nonadecadiene-2,3-dicarboxylic acid (2) have been described. Chemoselective carbon[bond]carbon S(N)2' coupling reactions of appropriate Grignard reagents with dimethyl bromomethylfumarate (7) in diethyl ether in the presence of HMPA at room temperature furnished the corresponding diesters 8 and 15 in 60-62% yields. The formed diesters 8 and 15 on hydrolysis gave respectively the corresponding desired diacids 9 and 2 in quantitative yields. Acetic anhydride induced ring closure of diacids 9 and 2 respectively gave the chaetomellic acid A anhydride (1) and isochaetomellic acid B anhydride (16) with 38-39% overall yields in five steps.     

Vibronic coupling in the excited cationic states of ethylene: simulation of the photoelectron spectrum between 12 and 18 eV

The effect of vibronic coupling on structure and spectroscopy is investigated in the excited cationic states of ethylene. It is found from equation of motion coupled cluster singles and doubles method for ionization potential electronic structure calculations in a triple-zeta plus double polarization basis set that ethylene in its third (B (2)A(g)) and fourth (C (2)B(2u)) ionized states does not have a stable minimum-energy geometry. The potential-energy surfaces of these states are energetically distinct and well separated at the ground-state geometry of ethylene, but in a geometry optimization as the structure of the ion relaxes, these surfaces end up in conical intersections and finally in the stable equilibrium geometry of the second ionized state (A (2)B(3g)). The topology of the potential-energy surfaces can be clearly understood using a vibronic model Hamiltonian. Furthermore, by diagonalizing this model Hamiltonian, the photoelectron spectrum of ethylene corresponding to the second, third, and fourth ionized states (12-18 eV) is simulated. Spectra from vibronic simulations including up to quartic coupling constants and using various normal-mode basis sets are compared to those from vertical Franck-Condon simulations to understand the importance of vibronic coupling and nonadiabatic effects and to examine the influence of individual normal modes on the spectrum.     

Synthesis of naturally occurring bioactive butyrolactones: maculalactones A-C and nostoclide I

Starting from citraconic anhydride (13), a simple multistep (9-10 steps) synthesis of naturally occurring butyrolactones maculalactone A (3), maculalactone B (1), maculalactone C (2) and nostoclide I (4) have been described with good overall yields via dibenzylmaleic anhydride (20) and benzylisopropylmaleic anhydride (27). The two anhydrides 20 and 27 were prepared by S_N2′ coupling reactions of appropriate Grignard reagents with dimethyl bromomethylfumarate (14), LiOH-induced hydrolysis of esters to acids, bromination of carbon-carbon double bond, in situ dehydration followed by dehydrobromination and chemoselective allylic substitution of bromoatom in disubstituted anhydrides 19 and 26 with appropriate Grignard reagents. The NaBH₄ reduction of these anhydrides 20 and 27 furnished the desired lactones 21 and 29, respectively. The lactone 21 on Knoevenagel condensation with benzaldehyde, furnished maculalactone B (1), which on isomerization gave maculalactone C (2). Selective catalytic hydrogenation of 1 gave maculalactone A (3). The conversion of lactone 29 to nostoclide I (4) is known.     

Chemical Composition of Essential Oil from Pilea microphylla and its Antimicrobial Activity

Chemistry of Natural Compounds -     

Cost Optimization Technique for Quantum Circuits

In this paper, an attempt is made to present a method of quantum cost minimization or optimization technique for quantum reversible circuits using proposed merger rules in Exclusive Sum of Product (ESOP) method. These modified ESOP methods are used to minimize the quantum circuits. We found that the quantum cost is drastically decreased than the previous ESOP method. It will be easy to find the quantum cost and quantum gate optimized quantum circuits implementation. It will also reduce quantum error while the quantum circuit is executed in real quantum processor.